Prof. Dr. MUSTAFA KÖMÜR
- Yöksis ID 138778
- Researcher ID
- ORCID ID 0000-0001-6453-7323
- Scopus ID
- Scholar ID
- E-posta mustafakomur@mersin.edu.tr
- Dahili Telefon
Birim
TIP FAKÜLTESİ
DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
ÇOCUK SAĞLIĞI VE HASTALIKLARI ANABİLİM DALI
DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
ÇOCUK SAĞLIĞI VE HASTALIKLARI ANABİLİM DALI
ÜAK Temel Alan Bilgisi
Sağlık Bilimleri Temel Alanı
Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
Çocuk Nörolojisi (Çocuk Sağlığı ve Hastalıkları)
Son 5 Makale
Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients
NEUROMUSCULAR DISORDERS, vol. 53, no. , pp. 105423– Link 2025
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort
FRONTIERS IN NEUROLOGY, vol. 16, no. , pp. 1–13 Link 2025
Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study
Seizure: European Journal of Epilepsy, vol. 123, no. , pp. 17–25 Link 2024
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study
CEREBELLUM, vol. 23, no. 5, pp. 1950–1965 Link 2024
Two Sibling Cases of Spastic Paraplegia-45 with a Novel Pathogenic Variant in NT5C2 Gene: Concomitant RYR1 Gene in One Sibling
MOLECULAR SYNDROMOLOGY, vol. 15, no. 4, pp. 1–6 Link 2024
NEUROMUSCULAR DISORDERS, vol. 53, no. , pp. 105423– Link 2025
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort
FRONTIERS IN NEUROLOGY, vol. 16, no. , pp. 1–13 Link 2025
Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study
Seizure: European Journal of Epilepsy, vol. 123, no. , pp. 17–25 Link 2024
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study
CEREBELLUM, vol. 23, no. 5, pp. 1950–1965 Link 2024
Two Sibling Cases of Spastic Paraplegia-45 with a Novel Pathogenic Variant in NT5C2 Gene: Concomitant RYR1 Gene in One Sibling
MOLECULAR SYNDROMOLOGY, vol. 15, no. 4, pp. 1–6 Link 2024
Son 5 Bildiri
A national plan of action to raise awareness and improve medical care of Duchenne muscular Dystrophy (AIM-DMD)
29th World Muscle Society Congress Prague, Czechia, 2024 (06.10.2024 - ) Link 2024
Ebstein-Barr Virüse Bağlı Alice Harikalar Diyarında Sendromu, 4. Kranial Sinir Paralizisi
17. Ulusal Çocuk Enfeksiyon Hastalıkları ve Bağışıklama Kongresi (11.02.2024 - ) 2024
Eşlik eden başka bulguları olan veya sendromik kombine İmmün yetmezlikler] Geç tanı alan DİGEORGE Sendromlu olgu; Nöropsikyatrik bulgular uyarıcı olabilir!
10. Klinik İmmünoloji Kongresi (15.04.2024 - 18.04.2024) Link 2024
Benign Ailesel Makrosefalisi Olan Çocukların Denver II Sonuçları
8. GENÇ PEDİATRİSTLER KONGRSİ (02.11.2023 - ) 2023
Developmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic Diagnosis
17th International Child Neurology Congress (03.10.2022 - 07.10.2022) Link 2022
29th World Muscle Society Congress Prague, Czechia, 2024 (06.10.2024 - ) Link 2024
Ebstein-Barr Virüse Bağlı Alice Harikalar Diyarında Sendromu, 4. Kranial Sinir Paralizisi
17. Ulusal Çocuk Enfeksiyon Hastalıkları ve Bağışıklama Kongresi (11.02.2024 - ) 2024
Eşlik eden başka bulguları olan veya sendromik kombine İmmün yetmezlikler] Geç tanı alan DİGEORGE Sendromlu olgu; Nöropsikyatrik bulgular uyarıcı olabilir!
10. Klinik İmmünoloji Kongresi (15.04.2024 - 18.04.2024) Link 2024
Benign Ailesel Makrosefalisi Olan Çocukların Denver II Sonuçları
8. GENÇ PEDİATRİSTLER KONGRSİ (02.11.2023 - ) 2023
Developmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic Diagnosis
17th International Child Neurology Congress (03.10.2022 - 07.10.2022) Link 2022